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Pharmacokinetics, urinary excretion and plasma protein binding of danofloxacin following intravenous administration in buffalo calves (Bubalus bubalis)
Pharmacokinetics, urinary excretion and plasma protein binding of danofloxacin was investigated in buffalo calves following intravenous administration at the dose rate of 1.25 mg/kg to select the optimal dosage regimen of danofloxacin. Drug concentrations in plasma and urine were measured by microbi...
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Published in: | Veterinary research communications 2009-10, Vol.33 (7), p.659-667 |
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description | Pharmacokinetics, urinary excretion and plasma protein binding of danofloxacin was investigated in buffalo calves following intravenous administration at the dose rate of 1.25 mg/kg to select the optimal dosage regimen of danofloxacin. Drug concentrations in plasma and urine were measured by microbiological assaying. In vitro plasma protein binding was determined employing the equilibrium dialysis technique. The distribution and elimination of danofloxacin were rapid, as indicated by values (mean ±SD) of distribution half-life (t₁/₂α = 0.16 ± 0.07 h) and elimination half-life (t₁/₂β = 4.24 ± 1.78 h), respectively. Volume of distribution at steady state (Vss) = 3.98 ± 1.69 L/kg indicated large distribution of drug. The area under plasma drug concentration versus time curve (AUC) was 1.79 ± 0.28 μg/mlxh and MRT was 8.64 ± 0.61 h. Urinary excretion of danofloxacin was 23% within 48 h of its administration. Mean plasma protein binding was 36% at concentrations ranging from 0.0125 μg/ml to 1 μg/ml. On the basis of pharmacokinetic parameters obtained, it is concluded that the revision of danofloxacin dosage regimen in buffalo calves is needed because the current dosage schedule (1.25 mg/kg) is likely to promote resistance. |
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Drug concentrations in plasma and urine were measured by microbiological assaying. In vitro plasma protein binding was determined employing the equilibrium dialysis technique. The distribution and elimination of danofloxacin were rapid, as indicated by values (mean ±SD) of distribution half-life (t₁/₂α = 0.16 ± 0.07 h) and elimination half-life (t₁/₂β = 4.24 ± 1.78 h), respectively. Volume of distribution at steady state (Vss) = 3.98 ± 1.69 L/kg indicated large distribution of drug. The area under plasma drug concentration versus time curve (AUC) was 1.79 ± 0.28 μg/mlxh and MRT was 8.64 ± 0.61 h. Urinary excretion of danofloxacin was 23% within 48 h of its administration. Mean plasma protein binding was 36% at concentrations ranging from 0.0125 μg/ml to 1 μg/ml. On the basis of pharmacokinetic parameters obtained, it is concluded that the revision of danofloxacin dosage regimen in buffalo calves is needed because the current dosage schedule (1.25 mg/kg) is likely to promote resistance.</description><identifier>ISSN: 0165-7380</identifier><identifier>EISSN: 1573-7446</identifier><identifier>DOI: 10.1007/s11259-009-9215-6</identifier><identifier>PMID: 19296232</identifier><language>eng</language><publisher>Dordrecht: Dordrecht : Springer Netherlands</publisher><subject>Animals ; antimicrobial agents ; Biomedical and Life Sciences ; blood plasma ; blood proteins ; Blood Proteins - metabolism ; Buffaloes ; calves ; danofloxacin ; dosage ; drug excretion ; Fluoroquinolones - administration & dosage ; Fluoroquinolones - blood ; Fluoroquinolones - pharmacokinetics ; Fluoroquinolones - urine ; half life ; Injections, Intravenous ; intravenous injection ; Kinetics ; Life Sciences ; Male ; Original Article ; pharmacokinetics ; Protein Binding ; quinolones ; urine ; veterinary drugs ; Veterinary Medicine/Veterinary Science ; Zoology</subject><ispartof>Veterinary research communications, 2009-10, Vol.33 (7), p.659-667</ispartof><rights>Springer Science+Business Media B.V. 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-9fe99bf73ac4a6e53120bcfcca1e5344f459dea9a5f886d057d44c353c7749513</citedby><cites>FETCH-LOGICAL-c394t-9fe99bf73ac4a6e53120bcfcca1e5344f459dea9a5f886d057d44c353c7749513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19296232$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sappal, Ravinder</creatorcontrib><creatorcontrib>Chaudhary, Rakesh Kumar</creatorcontrib><creatorcontrib>Sandhu, Harpal Singh</creatorcontrib><creatorcontrib>Sidhu, Pritam Kaur</creatorcontrib><title>Pharmacokinetics, urinary excretion and plasma protein binding of danofloxacin following intravenous administration in buffalo calves (Bubalus bubalis)</title><title>Veterinary research communications</title><addtitle>Vet Res Commun</addtitle><addtitle>Vet Res Commun</addtitle><description>Pharmacokinetics, urinary excretion and plasma protein binding of danofloxacin was investigated in buffalo calves following intravenous administration at the dose rate of 1.25 mg/kg to select the optimal dosage regimen of danofloxacin. Drug concentrations in plasma and urine were measured by microbiological assaying. In vitro plasma protein binding was determined employing the equilibrium dialysis technique. The distribution and elimination of danofloxacin were rapid, as indicated by values (mean ±SD) of distribution half-life (t₁/₂α = 0.16 ± 0.07 h) and elimination half-life (t₁/₂β = 4.24 ± 1.78 h), respectively. Volume of distribution at steady state (Vss) = 3.98 ± 1.69 L/kg indicated large distribution of drug. The area under plasma drug concentration versus time curve (AUC) was 1.79 ± 0.28 μg/mlxh and MRT was 8.64 ± 0.61 h. Urinary excretion of danofloxacin was 23% within 48 h of its administration. Mean plasma protein binding was 36% at concentrations ranging from 0.0125 μg/ml to 1 μg/ml. On the basis of pharmacokinetic parameters obtained, it is concluded that the revision of danofloxacin dosage regimen in buffalo calves is needed because the current dosage schedule (1.25 mg/kg) is likely to promote resistance.</description><subject>Animals</subject><subject>antimicrobial agents</subject><subject>Biomedical and Life Sciences</subject><subject>blood plasma</subject><subject>blood proteins</subject><subject>Blood Proteins - metabolism</subject><subject>Buffaloes</subject><subject>calves</subject><subject>danofloxacin</subject><subject>dosage</subject><subject>drug excretion</subject><subject>Fluoroquinolones - administration & dosage</subject><subject>Fluoroquinolones - blood</subject><subject>Fluoroquinolones - pharmacokinetics</subject><subject>Fluoroquinolones - urine</subject><subject>half life</subject><subject>Injections, Intravenous</subject><subject>intravenous injection</subject><subject>Kinetics</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Original Article</subject><subject>pharmacokinetics</subject><subject>Protein Binding</subject><subject>quinolones</subject><subject>urine</subject><subject>veterinary drugs</subject><subject>Veterinary Medicine/Veterinary Science</subject><subject>Zoology</subject><issn>0165-7380</issn><issn>1573-7446</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9Uctu1DAUtRCITgsfwAYsViAR8DOOl1CVh1QJJOjaunHswSWxBzsp5Uv4XRwyUnesrnzP48rnIPSEkteUEPWmUMqkbgjRjWZUNu09tKNS8UYJ0d5HO0Jb2SjekRN0Wso1qcSO8IfohGqmW8bZDv358h3yBDb9CNHNwZZXeMkhQv6N3a3NdZUihjjgwwhlAnzIaXYh4j7EIcQ9Th4PEJMf0y3YuvdpHNOvFQlxznDjYloKhmEKMZS6-Oe36hfvYUzYwnjjCn7xbulhrMx-naG8fIQeVLy4x8d5hq7eX3w7_9hcfv7w6fztZWO5FnOjvdO694qDFdA6ySkjvfXWAq0PIbyQenCgQfquawci1SCE5ZJbpYSWlJ-h55tv_djPxZXZXKclx3rSMCU6TZXsKoluJJtTKdl5c8hhqhkZSszahNmaMDVgszZh2qp5ejRe-skNd4pj9JXANkKpUNy7fHf5f67PNpGHZGCfQzFXXxmhvFbdUSoE_wuZKaDv</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Sappal, Ravinder</creator><creator>Chaudhary, Rakesh Kumar</creator><creator>Sandhu, Harpal Singh</creator><creator>Sidhu, Pritam Kaur</creator><general>Dordrecht : Springer Netherlands</general><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20091001</creationdate><title>Pharmacokinetics, urinary excretion and plasma protein binding of danofloxacin following intravenous administration in buffalo calves (Bubalus bubalis)</title><author>Sappal, Ravinder ; 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Drug concentrations in plasma and urine were measured by microbiological assaying. In vitro plasma protein binding was determined employing the equilibrium dialysis technique. The distribution and elimination of danofloxacin were rapid, as indicated by values (mean ±SD) of distribution half-life (t₁/₂α = 0.16 ± 0.07 h) and elimination half-life (t₁/₂β = 4.24 ± 1.78 h), respectively. Volume of distribution at steady state (Vss) = 3.98 ± 1.69 L/kg indicated large distribution of drug. The area under plasma drug concentration versus time curve (AUC) was 1.79 ± 0.28 μg/mlxh and MRT was 8.64 ± 0.61 h. Urinary excretion of danofloxacin was 23% within 48 h of its administration. Mean plasma protein binding was 36% at concentrations ranging from 0.0125 μg/ml to 1 μg/ml. On the basis of pharmacokinetic parameters obtained, it is concluded that the revision of danofloxacin dosage regimen in buffalo calves is needed because the current dosage schedule (1.25 mg/kg) is likely to promote resistance.</abstract><cop>Dordrecht</cop><pub>Dordrecht : Springer Netherlands</pub><pmid>19296232</pmid><doi>10.1007/s11259-009-9215-6</doi><tpages>9</tpages></addata></record> |
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subjects | Animals antimicrobial agents Biomedical and Life Sciences blood plasma blood proteins Blood Proteins - metabolism Buffaloes calves danofloxacin dosage drug excretion Fluoroquinolones - administration & dosage Fluoroquinolones - blood Fluoroquinolones - pharmacokinetics Fluoroquinolones - urine half life Injections, Intravenous intravenous injection Kinetics Life Sciences Male Original Article pharmacokinetics Protein Binding quinolones urine veterinary drugs Veterinary Medicine/Veterinary Science Zoology |
title | Pharmacokinetics, urinary excretion and plasma protein binding of danofloxacin following intravenous administration in buffalo calves (Bubalus bubalis) |
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